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HRID 530765作成日:2026年10月25日

Ethanol → 7-acetyl-12-[4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl]-7H-dibenzo [a,g]carbazole

https://huagongshe.com/reaction/530765

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Potassium CarbonateHCID 11430—
反応物4-(1-Phenyl-1H-benzimidazol-2-yl)phenylboronic AcidHCID 53249779—
反応物7-acetyl-12-bromo-7H-dibenzo [a,g]carbazoleHCID 71277894—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物7-acetyl-12-[4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl]-7H-dibenzo [a,g]carbazoleHCID 7127825990.9%

反応手順

Following the above procedure, Suzuki coupling of 3.4 g of 7-acetyl-12-bromo-7H-dibenzo [a,g]carbazole and 3.8 g of 4-(1-phenyl-1H-benzo [d]imidazol-2-yl) phenylboronic acid were stirred together in 30 ml of toluene. To this was added 0.01 g of tetrakis(triphenylphosphine)palladium, 2.7 g of potassium carbonate and 10 ml of aqueous ethanol were added and refluxed under nitrogen for 6 h. The reaction was quenched with water and the toluene layer was removed and passed through a celite column. The organic layers were combined and then evaporated in a rotary evaporator under vacuum to yield 4.6 g of 7-acetyl-12-[4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl]-7H-dibenzo [a,g]carbazole as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09353085B2
出典データセットuspto-grants-2016_05
ORD IDord-6113bb22f8114640b99d78649f2a6266
出典メモuspto-grants-2016_05